Canonical Allele Identifier: CA1409910182
Gene: AGTR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148741804C= , CM000665.2:g.148741804C= GRCh38
NC_000003.11:g.148459591C= , CM000665.1:g.148459591C= GRCh37
NC_000003.10:g.149942281C= NCBI36
NG_008468.1:g.48934C=

Transcript Alleles

HGVS Amino-acid change
ENST00000349243.8:c.769C= MANE Select ENSP00000273430.3:p.Gln257=
ENST00000402260.2:c.769C= ENSP00000385641.3:p.Gln257=
ENST00000418473.7:c.769C= ENSP00000398832.4:p.Gln257=
ENST00000349243.7:c.769C= ENSP00000273430.3:p.Gln257=
ENST00000402260.1:c.856C= ENSP00000385641.2:p.Gln286=
ENST00000404754.2:c.769C= ENSP00000385612.2:p.Gln257=
ENST00000418473.6:c.874C= ENSP00000398832.3:p.Gln292=
ENST00000461609.1:c.769C= ENSP00000418851.1:p.Gln257=
ENST00000474935.5:c.769C= ENSP00000418084.1:p.Gln257=
ENST00000475347.5:c.769C= ENSP00000419783.1:p.Gln257=
ENST00000497524.5:c.769C= ENSP00000419422.1:p.Gln257=
NM_000685.4:c.769C= NP_000676.1:p.Gln257=
NM_004835.4:c.874C= NP_004826.5:p.Gln292=
NM_009585.3:c.769C= NP_033611.1:p.Gln257=
NM_031850.3:c.874C= NP_114038.4:p.Gln292=
NM_032049.3:c.856C= NP_114438.2:p.Gln286=
NM_000685.5:c.769C= MANE Select NP_000676.1:p.Gln257=
NM_001382736.1:c.769C= NP_001369665.1:p.Gln257=
NM_001382737.1:c.769C= NP_001369666.1:p.Gln257=
NM_004835.5:c.769C= NP_004826.6:p.Gln257=
NM_009585.4:c.769C= NP_033611.1:p.Gln257=
NM_031850.4:c.769C= NP_114038.5:p.Gln257=
NM_032049.4:c.769C= NP_114438.3:p.Gln257=